Medication info

Hanol Talniflumate Tablet

Prescription medicationTabletOralExpired
Ingredient · strength
Talniflumate›370mg / 1 tablet
Manufacturer / importer
Hanol Biopharma Co., Ltd.
Appearance
Pale yellow round film-coated tablets
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Expired

MFDS item code 200400376 · Notified 2004.07.09

This product's status changed to Expired on 2024.04.01. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of arthritis (including rheumatoid arthritis)
Who takes it
Adults
Adult dose
Administer talniflumate 370 mg orally 3 times daily. For severe cases, administer 740 mg per dose. The dose may be adjusted according to age and symptoms.

Ingredients

Manufacturer
Hanol Biopharma Co., Ltd.

Efficacy & effects

Treatment of arthritis (including rheumatoid arthritis)

  • Rheumatoid arthritis
  • osteoarthritis
  • degenerative joint disease
View approved original text

This medication is used for the treatment of rheumatoid arthritis and osteoarthritis (degenerative joint disease). Rheumatoid arthritis is an autoimmune disease that causes inflammation and pain in the joints, while osteoarthritis is a degenerative disease that causes pain and functional impairment due to damage to joint cartilage. This drug helps to relieve the symptoms of these joint diseases and improve joint function.

How to take

Adult dose

Administer talniflumate 370 mg orally 3 times daily. For severe cases, administer 740 mg per dose. The dose may be adjusted according to age and symptoms.

Precautions

This medication should be used with caution in patients who regularly consume more than three drinks a day due to the risk of gastrointestinal bleeding; consultation with a physician or pharmacist is essential. This medication may increase the risk of cardiovascular disease; patients with a history or risk factors of heart disease should be especially careful and notify medical personnel immediately if cardiovascular symptoms occur. This drug can cause serious gastrointestinal adverse reactions, including gastrointestinal bleeding, ulcers, and perforation, thus elderly patients or those with a history of gastrointestinal diseases should use it cautiously. Patients with peptic ulcers, those allergic to the ingredients of this medication, and severe liver, kidney, or heart disease patients, as well as pregnant or nursing women, should not use this drug. Patients with impaired liver or kidney function, elderly patients, and those taking diuretics should use this drug cautiously and monitor their condition through regular checks. This medication may cause gastrointestinal symptoms such as nausea, vomiting, diarrhea, abdominal pain, and can rarely lead to skin rashes, hives, cardiovascular symptoms, and renal function abnormalities; consult medical personnel immediately if any unusual symptoms occur. This medication should be administered at the minimal effective dose for the shortest duration, and regular blood tests and liver and kidney function checks are important for long-term use. It is advisable not to take this medication with other non-steroidal anti-inflammatory drugs, and it may interact with certain blood pressure medications, diuretics, anticoagulants, lithium, methotrexate, so patients should inform their healthcare provider of any medications they are currently taking. Pregnant women, especially in the later stages of pregnancy, should avoid this medication as it may harm the fetus, and breastfeeding mothers should decide on its use considering the potential transmission of the drug through breast milk and the infant's safety. This medication is not safe for children, particularly those under 12 years of age, and due to the high risk of side effects, elderly patients should be extra careful. Store this medication out of the reach of children, and it is important for quality and safety not to transfer it to a different container.

Side effects

  • Gastrointestinal bleeding
  • cardiovascular thrombotic reactions
  • myocardial infarction
  • stroke
  • nausea
  • vomiting
  • photosensitivity
  • asthma attacks
  • systemic malaise due to hypotension
  • hypersensitivity shock
Show 33 more
  • diarrhea
  • abdominal distension
  • constipation
  • dyspepsia
  • ulcerative stomatitis
  • abdominal pain
  • hematemesis
  • colitis
  • exacerbation of Crohn's disease
  • hypertension
  • tachycardia
  • chest pain
  • arrhythmia
  • palpitations
  • hypotension
  • congestive heart failure
  • edema
  • hypertension
  • heart failure
  • vesicular reactions
  • Stevens-Johnson syndrome
  • Lyell syndrome
  • rash
  • urticaria
  • pruritus
  • purpura
  • dizziness
  • acute renal failure
  • interstitial nephritis
  • nephrotic syndrome
  • fluoride poisoning
  • abnormal liver function tests
  • thrombocytopenia

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly sealed container to prevent air or moisture from entering and kept at room temperature between 1 to 30 degrees Celsius. Storing it this way helps maintain the effectiveness of the medication and prevents deterioration.

Appearance and packaging

Appearance

Pale yellow round film-coated tablets

Package unit

30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

No questions yet.

For anything that needs medical judgment, consult a doctor or pharmacist.

Related searches

Search tags

Suggested searches

This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.